重组人心型脂肪酸结合蛋白/脂肪酸结合蛋白3蛋白-分析方法-资讯-生物在线

重组人心型脂肪酸结合蛋白/脂肪酸结合蛋白3蛋白

作者:上海信裕生物科技有限公司 2023-04-25T00:00 (访问量:1092)

 重组人心型脂肪酸结合蛋白/脂肪酸结合蛋白3蛋白

英文名称 Recombinant human FABP3 protein, His
中文名称 重组人心型脂肪酸结合蛋白/脂肪酸结合蛋白3蛋白
别    名 MDGI; FABP11; H-FABP; M-FABP; O-FABP; Fatty acid-binding protein, heart; Fatty Fatty acid-binding protein 3; Heart-type fatty acid-binding protein (H-FABP); Mammary-derived growth inhibitor (MDGI); Muscle fatty acid-binding protein (M-FABP); FABPH_HUMAN; Cardiac FABP; Recombinant human FABP3 protein, His  
理论分子量 15kDa
检测分子量 15-17 kDa
性    状 Lyophilized or Liquid
浓    度 >0.5 mg/ml
物    种 Human
序    列 2-133/133
纯    度 >95% as determined by SDS-PAGE
纯化方法 AC
内毒素 Not analyzed
表达系统 E.coli
活性 Not tested
标签 His
缓 冲 液 20 mM Tris-HCl (pH=8.0) with 150 mM NaCl and 100 mM imidazole
保存条件 Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍 Fatty acid-binding proteins, designated FABPs, are a family of homologous cytoplasmic proteins that are expressed in a highly tissue-specific manner and play an integral role in the balance between lipid and carbohydrate metabolism. FABPs mediate fatty acid (FA) and/or hydrophobic ligand uptake, transport and targeting within their respective tissues. The mechanisms underlying these actions can give rise to both passive diffusional uptake and protein-mediated transmembrane transport of FAs. FABPs are expressed in adipocytes (A-FABP), brain (B-FABP), epidermis (E-FABP, also designated psoriasis-associated FABP or PA-FABP), muscle and heart (H-FABP, also designated mammary-derived growth inhibitor or MDGI), intestine (I-FABP), liver (L-FABP), myelin (M-FABP) and testis (T-FABP). MDGI is highly expressed in the myocardium, skeletal and smooth muscle fibers, lipid and/or steroid synthesizing cells and terminally differentiated epithelia of the respiratory, intestinal and urogenital tracts.
 
产品图片
The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.
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